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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 1
2006 1
2007 1
2008 1
2009 1
2010 1
2013 1
2014 4
2015 5
2016 4
2017 4
2018 6
2019 2
2020 3
2021 5
2022 3
2023 3
2024 1

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44 results

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Page 1
Early spinal muscular atrophy treatment following newborn screening: A 20-month review of the first Italian regional experience.
Gagliardi D, Canzio E, Orsini P, Conti P, Sinisi V, Maggiore C, Santarsia MC, Lagioia G, Lupis G, Roppa I, Scianatico G, Mancini D, Corti S, Comi GP, Gentile M, Gagliardi D. Gagliardi D, et al. Among authors: orsini p. Ann Clin Transl Neurol. 2024 Apr 10. doi: 10.1002/acn3.52018. Online ahead of print. Ann Clin Transl Neurol. 2024. PMID: 38600653 Free article.
TNFRSF13B gene mutation in familial acute myeloid leukemia: A new piece in the complex scenario of hereditary predisposition?
Cumbo C, Orsini P, Tarantini F, Anelli L, Zagaria A, Tragni V, Coccaro N, Tota G, Parciante E, Conserva MR, Redavid I, Minervini CF, Minervini A, Attolico I, Gentile M, Pierri CL, Specchia G, Musto P, Albano F. Cumbo C, et al. Among authors: orsini p. Hematol Oncol. 2023 Dec;41(5):942-946. doi: 10.1002/hon.3212. Epub 2023 Aug 3. Hematol Oncol. 2023. PMID: 37534633
Case report: biallelic DNMT3A mutations in acute myeloid leukemia.
Cumbo C, Orsini P, Anelli L, Zagaria A, Iannò MF, De Cecco L, Minervini CF, Coccaro N, Tota G, Parciante E, Conserva MR, Redavid I, Tarantini F, Minervini A, Carluccio P, De Grassi A, Pierri CL, Specchia G, Musto P, Albano F. Cumbo C, et al. Among authors: orsini p. Front Oncol. 2023 Jun 28;13:1205220. doi: 10.3389/fonc.2023.1205220. eCollection 2023. Front Oncol. 2023. PMID: 37448520 Free PMC article.
The genomic analysis brings a new piece to the molecular jigsaw of idiopathic erythrocytosis.
Zagaria A, Tarantini F, Orsini P, Anelli L, Cumbo C, Coccaro N, Tota G, Minervini CF, Parciante E, Conserva MR, Redavid I, Ricco A, Attolico I, Specchia G, Musto P, Albano F. Zagaria A, et al. Among authors: orsini p. Exp Hematol Oncol. 2022 Aug 28;11(1):47. doi: 10.1186/s40164-022-00301-1. Exp Hematol Oncol. 2022. PMID: 36031623 Free PMC article.
12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature.
Recalcati MP, Catusi I, Garzo M, Redaelli S, Massimello M, Maitz SB, Gentile M, Ponzi E, Orsini P, Zilio A, Montaldi A, Calò A, Capra AP, Briuglia S, La Rosa MA, Grillo L, Romano C, Bianca S, Malacarne M, Busè M, Piccione M, Larizza L. Recalcati MP, et al. Among authors: orsini p. Genes (Basel). 2022 Apr 27;13(5):780. doi: 10.3390/genes13050780. Genes (Basel). 2022. PMID: 35627165 Free PMC article. Review.
Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.
Inchingolo AD, Patano A, Coloccia G, Ceci S, Inchingolo AM, Marinelli G, Malcangi G, Montenegro V, Laudadio C, Palmieri G, Bordea IR, Ponzi E, Orsini P, Ficarella R, Scarano A, Lorusso F, Dipalma G, Corsalini M, Gentile M, Venere DD, Inchingolo F. Inchingolo AD, et al. Among authors: orsini p. Medicina (Kaunas). 2021 Dec 10;57(12):1350. doi: 10.3390/medicina57121350. Medicina (Kaunas). 2021. PMID: 34946295 Free PMC article.
44 results